Design, Synthesis, and Pharmacology of a Highly Subtype-Selective GluR1/2 Agonist, (<i>RS</i>)-2-Amino-3-(4-chloro-3-hydroxy-5-isoxazolyl)propionic Acid (Cl-HIBO)Esben Jannik Bjerrum, Ulf Madsen, Anders S. Kristensen et al.|Journal of Medicinal Chemistry|2003Cited by 43
Tweaking Agonist Efficacy at N-Methyl-d-aspartate Receptors by Site-Directed MutagenesisKasper B. Hansen, Hans Bräuner‐Osborne, Jesper L. Kristensen et al.|Molecular Pharmacology|2005Cited by 28